Changeflow GovPing Pharma & Drug Safety Philips Radiology Device Safety Alert
Priority review Notice Amended Final

Philips Radiology Device Safety Alert

Favicon for ansm.sante.fr ANSM Drug & Device Safety Alerts
Published March 20th, 2026
Detected March 20th, 2026
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Summary

The French ANSM has been informed of a safety action initiated by Philips Medical Systems Nederland BV concerning radiology devices. Affected users have received a direct communication from the company regarding this action, registered under ANSM reference R2606927.

What changed

The French National Agency for Medicines and Health Products Safety (ANSM) has issued a safety alert regarding a specific action undertaken by Philips Medical Systems Nederland BV concerning their radiology interventionnel devices, including the RX Azurion, Allura Xper, Allura Centron, and Allura CV20 models. This alert, registered under reference R2606927, indicates that Philips has directly communicated with the affected users. The ANSM is providing this information to imaging and interventional radiology services.

Healthcare providers utilizing these Philips radiology devices should review the communication from Philips Medical Systems Nederland BV, which was provided on March 20, 2026. For any specific questions or concerns related to this safety action, direct contact with Philips Medical Systems Nederland BV is advised. The ANSM's role here is informational, highlighting the company-initiated safety measure.

What to do next

  1. Review Philips Medical Systems Nederland BV safety communication dated March 20, 2026.
  2. Contact Philips Medical Systems Nederland BV directly for any questions regarding the safety action.

Source document (simplified)

A+ A-

Information n° R2606927 destinée aux services d’imagerie et radiologie interventionnelle L'ANSM a été informée de la mise en œuvre d’une action de sécurité effectuée par la société Philips Medical Systems Nederland BV.

Les utilisateurs concernés ont reçu le courrier ci-joint.

Cette action de sécurité est enregistrée à l’ANSM sous le n° R2606927. Pour toute question, merci de vous adresser directement à l’émetteur de l’action de sécurité. Téléchargez le courrier de la société Philips Medical Systems Nederland BV (20/03/2026)

Source

Analysis generated by AI. Source diff and links are from the original.

Classification

Agency
ANSM
Published
March 20th, 2026
Instrument
Notice
Legal weight
Non-binding
Stage
Final
Change scope
Substantive
Document ID
Information n° R2606927

Who this affects

Applies to
Healthcare providers
Industry sector
3345 Medical Device Manufacturing
Activity scope
Medical Device Safety
Geographic scope
France FR

Taxonomy

Primary area
Medical Devices
Operational domain
Clinical Operations
Topics
Product Safety Healthcare Operations

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